C-terminal modification and functionalization of proteins via a self-cleavage tag triggered by a small molecule

Nat Commun. 2023 Nov 7;14(1):7169. doi: 10.1038/s41467-023-42977-x.

Abstract

The precise modification or functionalization of the protein C-terminus is essential but full of challenges. Herein, a chemical approach to modify the C-terminus is developed by fusing a cysteine protease domain on the C-terminus of the protein of interest, which could achieve the non-enzymatic C-terminal functionalization by InsP6-triggered cysteine protease domain self-cleavage. This method demonstrates a highly efficient way to achieve protein C-terminal functionalization and is compatible with a wide range of amine-containing molecules and proteins. Additionally, a reversible C-terminal de-functionalization is found by incubating the C-terminal modified proteins with cysteine protease domain and InsP6, providing a tool for protein functionalization and de-functionalization. Last, various applications of protein C-terminal functionalization are provided in this work, as demonstrated by the site-specific assembly of nanobody drug conjugates, the construction of a bifunctional antibody, the C-terminal fluorescent labeling, and the C-terminal transpeptidation and glycosylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cysteine / metabolism
  • Cysteine Proteases* / metabolism
  • Glycosylation
  • Protein C* / metabolism
  • Proteins / metabolism

Substances

  • Protein C
  • Proteins
  • Cysteine Proteases
  • Cysteine